中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A trans diacyloxylation of indoles

文献类型:期刊论文

作者Liu Q(刘强)1; Zhao QY(赵庆勇)1; Liu J(刘劼)1; Wu P(巫攀)1; Yi H(易宏)1; Lei AW(雷爱文)1,2
刊名Chemical Communications
出版日期2012
卷号48期号:26页码:3239-3241
ISSN号1359-7345
通讯作者雷爱文
英文摘要A trans diacyloxylation of indoles is accomplished by employing PhI(OAc)2 as the oxidant. A broad range of functional groups are well tolerated. Both the electronic properties of the N-protecting groups of indoles and the acidity of the reaction media play important roles in the selectivity of indole acyloxylation reactions.
学科主题物理化学与绿色催化
收录类别SCI
资助信息Program for Changjiang Scholars and Innovative Research Team in University (IRT1030);National Natural Science Foundation of China (20972118;20832003);financial support from Wuhan University
语种英语
WOS记录号WOS:000300874700029
公开日期2013-10-11
源URL[http://210.77.64.217/handle/362003/3805]  
专题兰州化学物理研究所_OSSO国家重点实验室
作者单位1.Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
2.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
推荐引用方式
GB/T 7714
Liu Q,Zhao QY,Liu J,et al. A trans diacyloxylation of indoles[J]. Chemical Communications,2012,48(26):3239-3241.
APA Liu Q,Zhao QY,Liu J,Wu P,Yi H,&Lei AW.(2012).A trans diacyloxylation of indoles.Chemical Communications,48(26),3239-3241.
MLA Liu Q,et al."A trans diacyloxylation of indoles".Chemical Communications 48.26(2012):3239-3241.

入库方式: OAI收割

来源:兰州化学物理研究所

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